- Trials with a EudraCT protocol (8,462)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (48)
8,462 result(s) found for: PL 1.
Displaying page 136 of 424.
| EudraCT Number: 2018-001618-13 | Sponsor Protocol Number: R475-OA-1816 | Start Date*: 2018-11-28 | ||||||||||||||||
| Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: Study to Evaluate Arthroplasty Specimens in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and Hip | ||||||||||||||||||
| Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-001269-18 | Sponsor Protocol Number: VMT-VT-1161-CL-011 | Start Date*: 2019-03-13 | |||||||||||
| Sponsor Name:Mycovia Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VT-1161 Oral Capsules in the Treatment of Subjects with Recurrent Vulvovaginal Candidiasis | |||||||||||||
| Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: BG (Completed) PL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003591-22 | Sponsor Protocol Number: FER-IBD-07-MAIN | Start Date*: 2008-10-30 | |||||||||||
| Sponsor Name:Vifor (International) Inc. | |||||||||||||
| Full Title: A multi-centre, randomised, prospective, single-blinded, controlled study to investigate the efficacy and safety of a standardised maintenance dosage regimen of intravenous ferric carboxymaltose (F... | |||||||||||||
| Medical condition: Iron deficiency anaemia in patients with inflammatory bowel disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) EE (Completed) ES (Completed) DK (Completed) GB (Completed) SE (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002160-22 | Sponsor Protocol Number: 0431-028 | Start Date*: 2004-11-17 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Safety of MK-0431 Monotherapy in Patients With Type 2 Diabetes Mellitus and Chronic Renal Insufficiency Who Have Inadequate Glycemic Co... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus Chronic Renal Insufficiency [MedDRA classification code: 10050441] | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001326-26 | Sponsor Protocol Number: AA-GYN-001 | Start Date*: 2007-08-14 | |||||||||||
| Sponsor Name:Omrix Biopharmaceuticals Ltd. | |||||||||||||
| Full Title: A Prospective, Controlled, Randomized, Multi-Center, Phase I/II Study Evaluating the Safety and Efficacy of Adhexil™ | |||||||||||||
| Medical condition: Patients that undergo surgery that involves the ovaries | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002588-24 | Sponsor Protocol Number: B1971060 | Start Date*: 2021-06-16 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PHASE 4, OPEN-LABEL, SINGLE-ARM TRIAL TO DESCRIBE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF TRUMENBA® WHEN ADMINISTERED TO IMMUNOCOMPROMISED PARTICIPANTS ≥10 YEARS OF AGE | |||||||||||||
| Medical condition: prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroup B | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003064-50 | Sponsor Protocol Number: HLX10-004-NSCLC303 | Start Date*: 2020-06-17 | |||||||||||
| Sponsor Name:Shanghai Henlius Biotech, Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multicenter, Phase III Clinical Study of HLX10 (Recombinant Anti-PD-1 Humanized Monoclonal Antibody Injection) + Chemotherapy (Carboplatin-Nanoparticle Albumin-Bound (na... | |||||||||||||
| Medical condition: First-Line Therapy for Locally Advanced or Metastatic Squamous Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002539-32 | Sponsor Protocol Number: The_WE_Study | Start Date*: 2015-03-23 | |||||||||||
| Sponsor Name:St. Olavs University Hospital | |||||||||||||
| Full Title: The WE Study - Walking Easier with cerebral palsy | |||||||||||||
| Medical condition: cerebral palsy | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) FR (Ongoing) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005019-29 | Sponsor Protocol Number: Rux-cALL-Pol_2020 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Medical University of Lodz | ||||||||||||||||||
| Full Title: Single-arm interventional study with ruxolitinib and AIOEP-BFM2017 chemotherapy in children with acute lymphoblastic leukemia and confirmed activation of JAK/STAT pathway. | ||||||||||||||||||
| Medical condition: Acute Lymphoblastic Leukemia with confirmed activating of JAK/STAT pathway in children and adolescents <18 years of age | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-001934-12 | Sponsor Protocol Number: SCD-044-19-16 | Start Date*: 2023-06-14 | |||||||||||
| Sponsor Name:Sun Pharmaceutical Industries Limited | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF SCD-044 IN THE TREATMENT OF MODERATE TO SEVERE ATOPIC DERMATITIS | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000413-20 | Sponsor Protocol Number: 3000-03-005/ENGOT-OV44/GSK213350 | Start Date*: 2018-11-07 | ||||||||||||||||
| Sponsor Name:TESARO, Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Phase 3 Comparison of Platinum-Based Therapy with TSR-042 and Niraparib Versus Standard of Care Platinum-Based Therapy as First-line Treatment of Stage III or IV Non-muc... | ||||||||||||||||||
| Medical condition: Stage 3 or 4 High Grade Non-mucinous epithelial ovarian cancer (serous, endometrial, clear cell, carcinosarcoma, and mixed pathologies) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FI (Trial now transitioned) BE (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) CZ (Trial now transitioned) FR (Trial now transitioned) GR (Trial now transitioned) PL (Trial now transitioned) NL (Ongoing) ES (Ongoing) NO (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-003053-42 | Sponsor Protocol Number: CNTO1959PSO3011 | Start Date*: 2018-09-04 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Placebo- and Active Comparator-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics (PK) of Subcutaneously Administered Guselkumab for the Trea... | |||||||||||||
| Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) NL (Ongoing) PL (Trial now transitioned) HU (Trial now transitioned) Outside EU/EEA IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001953-28 | Sponsor Protocol Number: EFC15804 | Start Date*: 2019-07-01 | |||||||||||
| Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Pivotal Study to Assess the Efficacy, Safety, and Tolerability of Dupilumab in Patients with Moderate-to-severe Chronic Obstr... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) DK (Completed) FI (Completed) CZ (Completed) HU (Completed) PL (Completed) SK (Completed) BG (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003086-34 | Sponsor Protocol Number: CAIN457A3301 | Start Date*: 2013-12-04 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A 52-week, multicenter, randomized, double-blind, placebo-controlled study of subcutaneous secukinumab to demonstrate efficacy as assessed by palmoplantar pustulosis Psoriasis Area and Severity Ind... | ||||||||||||||||||
| Medical condition: Moderate to severe chronic palmoplantar pustular psoriasis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Completed) GB (Completed) AT (Completed) ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-000362-42 | Sponsor Protocol Number: THR-687-002 | Start Date*: 2021-10-06 | ||||||||||||||||
| Sponsor Name:Oxurion NV | ||||||||||||||||||
| Full Title: A Phase 2, randomised, multicentre study to assess the dose level of multiple THR-687 injections and to evaluate the efficacy and safety of THR-687 versus aflibercept for the treatment of diabetic ... | ||||||||||||||||||
| Medical condition: Diabetic macular oedema (DME) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SK (Prematurely Ended) LT (Completed) LV (Prematurely Ended) HU (Prematurely Ended) PT (Prematurely Ended) DE (Ongoing) IT (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-002017-22 | Sponsor Protocol Number: 63723283LUC1001 | Start Date*: 2016-11-16 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A First-in-Human, Open-label, Phase 1/2 Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of JNJ-63723283, an Anti-PD-1 Monoclonal Antibody, in Subjects with A... | |||||||||||||
| Medical condition: Advanced Stage Solid Tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002791-18 | Sponsor Protocol Number: 0476-302 | Start Date*: 2006-09-28 | |||||||||||
| Sponsor Name:Suomen MSD Oy | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Double-Dummy, Parallel-Group Study Evaluating the Effects of 2 Different Regimens of Montelukast (Daily Dosing and Intermittent, Episode-Driven Dosing) Comp... | |||||||||||||
| Medical condition: episodic or intermittent asthma | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DK (Completed) DE (Completed) IT (Completed) LT (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003984-20 | Sponsor Protocol Number: LSK-AM301 | Start Date*: 2017-12-11 |
| Sponsor Name:Elevar Therapeutics, Inc | ||
| Full Title: A Prospective, Randomized, Double-Blinded, Placebo-Controlled, Multinational, Multicenter, Parallel-group, Phase III Study to Evaluate the Efficacy and Safety of Apatinib plus Best Supportive Care ... | ||
| Medical condition: Advanced or Metastatic Gastric Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) PL (Completed) FR (Completed) IT (Completed) RO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003028-34 | Sponsor Protocol Number: JAB-21822-1001 | Start Date*: 2022-02-25 | |||||||||||
| Sponsor Name:Jacobio Pharmaceuticals Co., Ltd. | |||||||||||||
| Full Title: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Evidence of Antitumor Activity of JAB-21822 Monotherapy and Combination Therapy i... | |||||||||||||
| Medical condition: Phase 1: Advanced solid tumors, relapsed or refractory to standard therapy Phase 2: non-small cell lung cancer, metastatic colorectal cancer, and other solid tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Completed) HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003153-15 | Sponsor Protocol Number: GS-US-419-4016 | Start Date*: 2017-08-01 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Efficacy and Safety of Filgotinib in the Treatment of Perianal Fistulizing Crohn’s Disease | |||||||||||||
| Medical condition: Perianal Fistulizing Crohn’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) CZ (Completed) DE (Completed) PL (Completed) ES (Completed) AT (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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